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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03237247
Other study ID # 17100256
Secondary ID
Status Completed
Phase N/A
First received July 22, 2017
Last updated August 7, 2017
Start date March 1, 2016
Est. completion date February 28, 2017

Study information

Verified date August 2017
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cases with extrahepatic cholestasis are common and faced during day to day clinical practice, however reaching the final etiology is sometimes challenging and needs investigations which are usually expensive, may carry hazards to the patients, or inaccessible so we are in need for a method which is easily available, affordable and safe for aiding in the differential diagnosis of extrahepatic cholestasis. our study aiming to evaluate the role of complete blood count in predicting the etiology of extrahepatic cholestasis.


Description:

Extrahepatic cholestasis has various etiologies including benign causes (benign stricture, chronic pancreatitis, choledochal cyst, mirizzi syndrome, etc...), choledocholithiasis, malignant causes (cancer pancreas, gallbladder cancer, cholangiocarcinoma, etc....), parasitic infestations (fasciola hepatica, ascaris lumbricoides, etc......) and other causes. it is essential to detect the exact cause of extrahepatic cholestasis in order to determine treatment options. diagnosing such conditions depends on clinical examination, laboratory investigations, imaging studies, endoscopic procedures, biopsy and even surgical intervention. some of these investigations are expensive, not available, or carry risk to the patients. moreover non of them is accurate 100%. Complete blood count is already available, easy to obtain, not invasive investigation. In these study we are trying to evaluate the role of complete blood count parameters namely RDW, MPV, PDW, PCT, NLR, PLR in the differential diagnosis of extrahepatic cholestasis.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date February 28, 2017
Est. primary completion date February 28, 2017
Accepts healthy volunteers
Gender All
Age group 14 Years and older
Eligibility Inclusion Criteria:

- patients with extrahepatic cholestasis

Exclusion Criteria:

- age under 14 years

- previous bilio-pancreatic interventions

- hemoglobinopathy

- splenomegaly

- myeloproliferative disorders

- diabetes mellitus

- recent blood transfusion in less than one month

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary differential diagnosis of extrahepatic cholestasis complete blood count parameters 10 days
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